On Determinants of Lens Regeneration
On Determinants of Lens Regeneration
批准号:
9288485
负责人:
Katia Del Rio-Tsonis
金额:
$36.13万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-09-01 至 2020-05-31
关键词:
AdultAgeAmphibiaAnimalsBiologyBody partCellsDevelopmentDorsalEnsureEphrin-B2EphrinsEpithelial CellsEventEyeFutureGene ExpressionGene Expression ProfileGene Expression ProfilingGene Expression RegulationGene Transfer TechniquesGenesGenomeGoalsIn VitroIrisMammalsMedicineMicroRNAsMolecularNTN1 geneNatural regenerationNewtsOrganOutcomePathway interactionsPatternPigmentsProcessRegulationResearchResourcesRoleScientistSideSignal TransductionSiteSolidSomatic CellSpecificitySystemTechniquesTissuesTranscriptVertebratescomparativeexperimental studyfascinatehistone modificationin vivoknock-downlenslens inductionlens regenerationloss of functionnoveloptic cupreceptorregenerativetissue regenerationtooltranscription factortranscriptometranscriptomicstransdifferentiation
中文摘要
点击翻译按钮获取中文摘要
英文摘要
PROJECT SUMMARY
When it comes to tissue regeneration in vertebrates the newts stand out as the champions.
These animals can regenerate many organs and body parts even as adults and of old age. Thus,
the newts could provide much coveted answers that the field of regenerative biology and
medicine seeks. Among all tissues that can be regenerated the lens is a classic case of
transdifferentiation because when removed as a whole regeneration ensues from a different
tissue, the iris. Interestingly only the dorsal side of the iris is capable for transdifferentiation and
not the ventral even though they both are made up of pigment epithelial cells. Thus, there must
exist fundamental differences between dorsal and ventral iris that allow regeneration from the
one site and not the other. Via transcriptomic analysis we have identified interesting patterns of
gene expression. Some of the genes that show high levels of expression in dorsal or ventral iris
will be examined in this proposal. In particular, we will examine the role of highly-regulated
transcriptional factors in dorsal or ventral iris in the induction process (specific aim 1). For
example, we have identified Tbx5 and Vax2 as dorsal- and ventral –specific respectively. Can the
ventral iris be induced if we knock-down Vax2 or up-regulate Tbx5? Also we have seen
interesting patterns of regulation of Ephrin-B2 and its receptor as well as of netrin-1 and its
receptor UNC5 (specific aim 2). Ephrin-B2 is highly expressed in the dorsal iris, while netrin-1
in the ventral iris, with their receptors having opposite patterns. Since these pairs are involved
in repulsion of cells we believe that they are involved in setting the boundaries between dorsal
and ventral iris and disallow mingling of dorsal and ventral iris cells, thus ensuring correct
regeneration. Moreover, it seems that Ephrin/netrin signaling is part of the Vax2/Tbx5 network,
implying that all these genes might establish a novel pathway, which regulates lens regeneration.
This will be investigated with gain- or loss-of-function experiments. Outcome of the proposed
experiments will provide firm answers as to mechanisms of regeneration and will allow us to
extend in other species with the ultimate goal to eventually induce lens regeneration in
mammals.
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